Leaving hospital following urostomy surgery

Transcription

Leaving hospital
following
urostomy surgery
Information to help you
live a full and productive
life with an ostomy
Table of contents
Living with your urostomy
3
Help at home and in your community
Taking care of your urostomy
Skin care and cleaning your stoma
4
Removing hair from around your stoma
4
Skin irritation and sensitivities
4
Preventing infection and avoiding leaks
5
Treatment for a urinary infection
5
Who to call for help
18
Making a follow-up appointment
with your surgeon
19
Purchasing ostomy supplies
19
Financial assistance and resources
19
Community supports and information
19
Resource lists and contacts
Step- by-step: Changing your pouch
One-piece pouching system
6
Two-piece pouching system
9
Disposing of used supplies
12
Living with your ostomy
Personal hygiene:
Bathing or having a shower
13
Other water activities
Ostomy supply manufactures
20
Local suppliers
20
Ostomy clothing and accessories
21
21
Community support groups
22
Glossary
23
13
Notes
24
Returning to work or school
13
Clothing
14
Nutrition and diet
14
Managing odor
14
Travel
14
Sexual activities and intimacy
15
Managing stress
16
2––Leaving hospital following urostomy surgery
Living with your urostomy
Undergoing ostomy surgery will result is some
changes to your life. With support and training on
how to take care of your ostomy, you will find that
life can be as full as it was before your surgery.
This booklet provides information to help you
learn to live with a urostomy.
Following your surgery, you will begin to recover
and become involved in the care of your ostomy.
Before you leave the hospital, your care team will
begin the process of teaching you how to take
care of your ostomy. The care and support that
you received in hospital will continue once you
are discharged home. Community nurses will
be arranged to visit you at home to continue on
with the teaching process. Be sure to ask your
hospital care team and your community nurse as
many questions as you need so that you feel as
comfortable as possible with your ostomy. Once
you are home, you may also find it helpful to
connect with an ostomy support group. Meeting
other people who have adjusted their lifestyles
after this surgery and have managed to return to
their regular activities can be reassuring.
Over time you will become more confident and
comfortable with caring for your urostomy. Most
people living with an urostomy can return to a full
and active life.
Leaving hospital following urostomy surgery––3
Taking care of your urostomy
Skin care and cleaning your stoma
Keeping your stoma and surrounding areas
clean is important. To clean the skin around
your stoma, all you need to use is warm water
and a washcloth, or good quality paper towels.
It is not necessary to use soap to clean the area
around your stoma. If you prefer to use soap, use
a very mild soap. Be sure to rinse the soap off the
skin around your stoma very well because any
soap film may keep your pouching system from
sticking and may cause skin irritation. Always
dry your skin well before putting on your new
pouching system.
Sometimes you may see a small amount of blood
on your cloth. The stoma tissue contains small
blood vessels and may bleed a small amount
when cleaned. If you notice any bleeding that
does not stop, you should contact your health
care provider.
Things to avoid
Avoid using soaps and cleansers with oils,
perfumes, or deodorants since these can
sometimes cause skin problems or keep your skin
barrier from sticking.
The stoma has no nerve endings, so you are not
able to feel if you are rubbing too hard. Use a
gentle touch when cleaning around your stoma –
do not scrub.
Do not use alcohol or any other harsh chemicals
to clean your skin or stoma. They may irritate your
skin. Do not use moistened wipes, baby wipes
or towelettes that contain lanolin or other oils.
These can interfere with the skin barrier sticking
and may irritate your skin.
Unless recommended, do not apply powders or
creams to the skin around your stoma because
they can keep your skin barrier from sticking.
Removing hair from around your stoma
Shaving or clipping excess hair around the stoma
in the direction of hair growth can help keep your
stoma clean and may limit skin irritation. You
may shave with an electric razor or dry shave
with an ‘ostomy skin barrier powder’ and safety
razor. Always wash the skin well with water after
shaving. To protect the stoma when shaving, place
an empty toilet paper roll over the stoma.
Skin irritation and sensitivities
The best way to limit skin irritation is by having
a well-fitted and comfortable pouching system.
Your Enterostomal Therapy (ET) nurse in the
hospital or health care professional will help
you choose the system that fits and works best
for you. It is also important for you to identify
any issues with your pouch and be aware when
something is wrong or if your pouch does not
fit properly.
The opening of your skin barrier should be no
more than 1/8 of an inch away from the edge of
your stoma. Measure your stoma once a week for
the first six to eight weeks after your surgery. Your
stoma shrinks while it is healing and you need to
keep measuring so you can make sure that the
opening in the skin barrier is the right size for your
stoma. Re-measure your stoma if any irritation
develops between the stoma and flange.
Check your skin and the back of your skin barrier
each time you change your pouching system.
You can use a mirror to check your skin under
the stoma. Look for any places where stool may
have leaked under the skin barrier and onto
your skin. When you apply your next pouching
system, these areas may need some extra
reinforcement with skin barrier strips, rings or
paste. Your Enterostomal Therapy (ET) nurse or
health care professional will advise you when this
is recommended. It is helpful to hold your skin
smooth as you put your pouching system on to
avoid wrinkles that may lead to leakage.
Preventing infection and avoiding leaks
(See the step-by-step instructions for changing
your pouch in this booklet on page 6).
Urinary infections can occur with an urostomy.
Signs of a urinary tract infection:
Sensitive skin
If your skin is sensitive, it is helpful to tell your
Enterostomal Therapy (ET) nurse or health care
professional. A skin patch test may be necessary
to see if you have any reaction to the different skin
barriers and tapes. Usually the ingredients in the
skin barriers do not cause skin irritation.
You will know if you are having a “reaction” to
the skin barrier or tape most of the time, because
you will see skin changes that match the shape of
the product. Inform your Enterostomal Therapy
(ET) nurse or health care professional so they
can determine the cause of the irritation and
recommend another product if needed.
Itching or burning under the skin barrier may
indicate that you have leakage, a skin rash, or
a skin infection. If you feel itching or burning,
remove your pouching system as soon as possible
to check your skin for irritation.
A stoma rarely becomes infected. The most
important thing is to protect the skin around your
stoma. The best way to prevent an infection is to
make sure the pouching system fits properly.
Always change your pouching system at the first
signs of leakage. Do not try to patch the pouching
system with tape or paste. Leaving a leaking
pouch on can cause skin irritation.
To prevent leaking, always empty your pouch
before it is half-full.
• Cloudy, concentrated urine
• Odor in urine
• Temperature
• Low back pain
Treatment for a urinary infection
In order to diagnose a urinary tract infection, a
urine sample needs to be tested. Your doctor or
Enterostomal Therapy (ET) nurse would take
the urine directly from the stoma by using a
sterile catheter.
To prevent urinary tract infections, drink at least
eight glasses of fluid each day and include either
pure cranberry juice, cranberry supplements or
vitamin C to keep urine acidic. Leaving hospital following urostomy surgery––5
Step-by-step:
Changing your one-piece pouching system
1. Organize your supplies
What you need:
• Pouch
• Measuring guide
• Scissors
• Marker
• Barrier ring (as required)
• Disposal bag to discard your used product
• Wet and dry cleaning cloths
2. Caring for your stoma & skin
• Gently cleanse your stoma and surrounding
skin with a wet, warm cloth. A mild soap
may be used as long as all skin is rinsed
well. Pat skin dry.
• Your stoma will be swollen after surgery.
It may take six to eight weeks for your
stoma to reduce to its permanent size.
• Y
our stoma should be light pink or red
in colour.
• Y
our stoma will be moist and may bleed
slightly when washed.
• The skin around your stoma should not
have any signs of redness or a rash.
3. M
easuring your stoma
• Measure your stoma using the measuring
guide - it is important that there is a small
amount of space between the cut opening and
stoma. This allows room for your stoma to
expand and pass urine through the opening.
• After a six-week period, measurement is
generally not required and pouches may be
precut in advance.
• It is recommended that you re-measure your
stoma every two to three months to be certain
that there have not been any changes.
4. Creating and applying a barrier ring
• Trace the pattern of your stoma onto the paper
backing of the pouch.
• Cut the pouch to match the pattern. Put your
fingers inside the pouch to avoid cutting
through the pouch.
• Remove the paper backing from the skin barrier
portion of the pouch and set aside.
• Gently stretch and apply the barrier ring around
the cut opening of the sticky side of the skin
barrier portion of the pouch (if using).
5. S
ecuring the pouch in place
• Place the skin barrier opening around your
stoma. Make sure the pouch is hanging in the
correct position, normally downward. Gently
press the barrier onto your skin. Remove the
remaining tape backing.
General guidelines
• With an urostomy pouch, make sure that
the “teardrop symbol” is not visible. This
indicates that the “tap” is closed. When the
“teardrop” symbol is visible, the tap is “tap”
is open.
• Empty the pouch when it is 1/3 to 1/2 full
of urine.
• The pouching system should be changed
two to three times a week during the first
six to eight weeks. Long -term, the system
is generally changed twice weekly. This will
vary with each individual.
• If you are going to attach your pouch to a
bedside drainage bottle or bag for nighttime,
use the adaptor to attach the pouching
system to straight drainage. Ensure the
“teardrop” symbol is visible, indicating the
“tap” is open (as described above).
Make sure you:
• Change your pouching system if there are
signs of leakage or if you feel a burning or
itchy sensation.
• Notify your Enterostomal Therapy (ET)
nurse or health care professional if you have
questions or concerns.
Step-by-step:
Changing your two-piece pouching system
1. Organize your supplies
What you need:
• Flange
• Pouch
• Measuring guide
• Scissors
• Marker
• Barrier ring (as required)
• Wet and dry cleaning cloths
• Disposal bag for your used product
2. Caring for your stoma & skin
• Gently cleanse your stoma and surrounding
skin with a wet, warm cloth. A mild soap
may be used as long as all skin is rinsed
well. Pat skin dry.
• Check your stoma and surrounding
skin condition.
• Your stoma will be swollen after surgery. It
may take six to eight weeks for your stoma
to reduce to its permanent size.
• Your stoma should be light pink or red
in color.
3. Measuring your stoma
• For the first six to eight weeks after surgery,
your stoma should be measured and the
opening in the flange adjusted accordingly.
It is important that there is a small amount of
space between the cut opening and stoma.
This allows room for your stoma to expand and
pass urine through the opening.
• After a six-week period, measurement is
generally not required and flanges may be
precut in advance.
• It is recommended that you re-measure every
two to three months to be certain that there
have not been any changes.
4. Creating and applying a barrier ring
• Trace the pattern of the stoma shape onto the
back of the flange.
• Cut the flange to match the pattern.
• Remove the clear plastic backing on the flange
and set the flange aside.
• Gently stretch and apply the barrier ring around
the cut opening of the sticky side of the flange –
if using.
5. R
emove remaining tape backing
• Place the skin barrier opening around your
stoma and press it gently onto your skin.
Remove the remaining tape backing.
• A mirror may be helpful to centre the flange.
6. Secure pouch in place
• With an urostomy pouch, make sure that the
“teardrop symbol” is not visible. This indicates
that the “tap” is closed. When the “teardrop”
symbol is visible, the tap is “tap” is open.
• Place the pouch onto the base ring of
the flange.
• Place your fingers under the flange for support
while attaching the pouch to the flange. Move
your fingers clock-wise.
• Gently tug downward on the pouch to make
sure it is attached securely.
• If you are going to attach your pouch to a
bedside drainage bottle or bag for nighttime,
use the adaptor to attach the pouching system
to straight drainage. Ensure the “teardrop”
symbol is visible, indicating the “tap” is open
(as described above).
General guidelines
• Empty the pouch when it is 1/3 to 1/2 full
of urine.
• The pouching system needs to be changed
two to three times a week during the first six
to eight weeks. Long-term, the system should
be changed twice weekly. This may vary with
each individual.
Make sure you:
• Change the complete system if there are visible
signs of leakage.
• Notify your Enterostomal Therapy (ET) nurse
or health care professional with any concerns
or questions.
Disposing of used supplies
Put your soiled pouching system into a regular
plastic bag or a disposal bag provided by your
ostomy supplies company. These bags can be
thrown away with your regular garbage.
Living with your ostomy
An ostomy should not affect your ability to
resume your lifestyle. Many people find they can
continue all of the activities that they enjoyed
before their illness and/or surgery.
It will take time before you will be physically and
emotionally ready to resume normal activity.
Allow yourself the recovery time. Be good to
yourself and take the extra time to regain your
strength and energy.
Personal hygiene: Bathing or
having a shower
You can shower or bathe with or
without your pouching system in place.
Pouching systems are waterproof. You
may find it convenient to plan your
pouching system change around your
shower or bath.
Water, soap or shampoo cannot harm or enter
your stoma. If the water pressure is very strong,
be careful not to let it hit your stoma directly. It
is a good habit to empty the pouch before you
shower, bathe or participating in other water
activities, such as swimming.
While swimming, you may want to consider
wearing tight “biking style” shorts to keep the
pouch close to your body and help keep it from
“floating.” Other options may include a swimming
belt or layering a tighter athletic style bathing suit
under a trunk style bathing suit.
After bathing or swimming, you may use a
towel or a hairdryer (on the coolest setting) to
dry the tape and cloth backing of the pouching
system. This can also help prevent skin irritation
from wetness.
You may find it helpful to wait approximately
an hour after changing your pouching system
before swimming.
Returning to work or school
Many people have concerns about returning to
work or school activities. “Will I smell? Will there
be noises? Will they see it? What if someone asks?”
These are common concerns.
Other water activities
Noises associated with your pouch are often
muffled by clothing. By placing an arm across your
stoma site, you can further muffle noises. Your
pouch should not be visible once you are fully
dressed.
It is important to check your pouching system
before and after you have exposed it to water
including activities such as swimming. If you are
in water for a long period, the pouching system
may start to loosen from your skin.
Remember, as a person you have not changed.
You have a surface change that has given you back
your health. The decision to share with others is
personal. You only need to tell people you have an
ostomy if you want to.
Pouching systems are waterproof. However, you
may feel more secure if you wear skin-friendly
tape around the edges of your skin barrier when
you are in the water.
Clothing
You can continue to wear the same clothing that
you wore before your ostomy surgery. Some
people may prefer wearing suspenders instead of
a belt, pants with pleats and patterned clothing.
A full, snug undergarment is recommended to
give support to the pouching system and create
a smooth line under your clothing. Snug-fitting
clothing can be worn without fear of harming the
stoma or interfering with stoma functioning.
Nutrition and diet
Having an urostomy is not
usually associated with a
highly restricted diet. You
should always be aware of
the importance of fluids and
drink at least eight glasses of
fluid each day.
Managing odour
Your pouch is designed to
control odour. When it is
secure and in place, there
should be no odour. Urine odour is a result of a
person’s body chemistry. If you have concerns,
here are some things that you can do to help
reduce any odor when changing your pouch:
• Use deodorizing tablets or liquids for
deodorizing the inside of the pouch
• Use neutralizing sprays or wicks to freshen
the bathroom
Travel
People with an ostomy travel just like anyone else.
Here are some travel tips:
• Carry identification with your medical contact
information, ostomy product codes and
Enterostomal Therapy (ET) nurse’s name and
phone number. Your ostomy chapter, ostomy
retailer or company will often carry ostomy
identification cards. Medical I.D. bracelets can
be ordered through most pharmacies across
Ontario or through www.diabeticdrugstore.com
• Identify local ostomy retails in the area where
you are traveling in case you need supplies. You
can check with your current supplier to see if
they have local retail locations in other areas.
• Bring double the amount of ostomy supplies
that you would normally require. Always carry
supplies in your hand luggage.
• Pre-cut your flanges or pouches in advance to
avoid the need to bring scissors.
• A letter from your Enterostomal Therapy nurse
or doctor outlining the medical reasons for
the ostomy supplies may be helpful to avoid
unnecessary questioning if you are travelling
through customs and immigration.
• Get a copy of the current directory of Englishspeaking physicians or ones who speak in your
preferred language in various cities abroad
who charge a standard fee. The International
Association for Medical Assistance to Travelers
publishes these types of directories.
Visit www.iamat.org.
• Make sure you have travel insurance.
• Do not keep supplies in a car in the summer
or winter. Heat and cold can interfere with the
ostomy adhesives.
• Take advantage of available bathroom facilities
to empty your pouch more frequently than you
normally would.
• Carry toilet tissues or pre-moistened fragrance
free wipes in case the restroom does not
have any.
• Carry an “emergency kit” containing: a sealable
bag, pre-cut flange, pouch, paste (optional),
individually packaged pre-moistened fragrance
free wipes or paper towel and a mirror. Check
your kit regularly to ensure that the items
are useable.
• In an emergency, you can empty your pouch
into a sealable bag or one with a twist tie until
it can be disposed of later.
• Learn to say “toilet” in more than one language.
• Drink at least six to eight glasses of noncaffeinated liquids each day.
• Plan your visits to the washroom on airplanes
to avoid peek times, such as after meals or
before landing.
Sexual activities and intimacy
It is common for people with an ostomy to have
concerns about resuming sexual activities. You
may wonder whether your sex life or relationship
with your partner will change. Fears of rejection,
odour, leakage, and performance are natural. It is
recommended that you share any concerns with
your partner. Understanding each other’s feelings
is a very important part of coping with an ostomy.
Your ostomy should not limit or curtail sexual
activity. Many people report that the experience
of their surgery and the knowledge that the illness
is treated has brought their families and loved
ones closer than they were before.
Before sexual activities, empty your pouch
to minimize any leakage. To help minimize
concerns about your ostomy, you may find
these items helpful - a frilly half-slip, crotch-less
undergarments, a tube top stretched over the
abdomen or cummerbund. During sexual activity,
you may want to experiment with different
positions to find the one that is most comfortable
for you and your partner.
You will need to speak with your surgeon if you
have difficulty achieving an erection, experience
an altered sex drive, pain with intercourse or have
any other concerns.
Managing stress
Coping with disease,
or dealing with the
stress of surgery means
dealing with a variety of
problems, including: pain,
uncertainty and fear about
the future; limitation in
physical ability; changes
in social relationships;
insecurity about physical
attractiveness or competence; negotiating and
communicating with a medical system that can
be confusing and intimidating. The following
discussion on stress and coping will help you
recognize if you are suffering from stress and learn
how to manage stress.
Identifying the signs of stress
Stress can cause physical, emotional and
behavioral disorders that can affect your health,
vitality, peace-of-mind, as well as personal and
professional relationships. Too much stress can
cause illnesses such as insomnia, backaches, or
headaches, and can contribute to potentially lifethreatening diseases like high blood pressure and
heart disease.
Common signs of stress:
•
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•
•
•
•
•
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Excessive fatigue / exhaustion
Muscle tension
Irritability / anger
Upset stomach
Nervousness / trembling
Sleeplessness
Cold, sweaty hands
Loss of, or increase in, appetite
Grinding teeth / clenching jaw
General body complaints such as weakness,
dizziness, headaches or pain in the back
or muscles
Tips for reducing or controlling stress:
Be realistic. If you feel overwhelmed by certain
activities, learn to say NO! Eliminate an activity
that is not necessary. You may be taking on more
responsibility than you can, or should handle. If
you meet resistance, give reasons why you are
making the changes. Be willing to listen to other’s
suggestions and be ready to compromise.
Shed the “superman/superwoman” urge. No
one is perfect; so do not expect perfection from
yourself or others. Ask yourself, “What really
needs to be done? How much can I do? Is the
deadline realistic? What adjustments can I
make?” Do not hesitate to ask for help if you
need it.
Meditate. Just 10 to 20 minutes of quiet reflection
may bring relief from chronic stress, as well as
increase your tolerance to stress. Use the time to
listen to music, relax, and try to think of pleasant
things or of nothing.
Visualize. Use your imagination and picture how
you can manage a stressful situation successfully.
Whether it is a business presentation or moving
to a new place, many people feel visual rehearsals
boost self-confidence and help them take a more
positive approach to a difficult task.
Take one thing at a time. For people experiencing
stress, an ordinary workload can seem
unbearable. The best way to cope with this feeling
of being overwhelmed is to take on one task at
a time.
Pick one urgent task and work on it. Once you
accomplish that task, choose the next one. The
positive feeling of “checking off” tasks is satisfying
and will be motivation to continue.
Hobbies. Take a break from your worries by doing
something you enjoy; whether it is gardening or
painting, schedule time for your interests.
Go easy with criticism. You may expect too much
of yourself and others. Try not to feel frustrated,
let down, disappointed or even “trapped” when
another person does not measure up. The “other
person” may be a spouse or child that you are
trying to change to suit you. Remember that
everyone is unique, and has their own virtues,
shortcomings, and right to develop as individuals.
Getting help for stress
Exercise. Regular exercise is a popular way to
relieve stress. Being physically active for 20 to 30
minutes benefits the body and the mind.
Healthy lifestyle. Good nutrition makes a
difference. Limit intake of caffeine and alcohol,
exercise, get enough rest and balance work
and play.
Help may be as close as a friend or spouse. If
you think that you or someone you know may be
under more stress than just dealing with a passing
difficulty, it may be helpful to talk with your
doctor, spiritual advisor, or employee assistance
professionals. They may suggest you visit with a
psychiatrist, psychologist, social worker, or other
qualified counselor.
Adapted from: National Mental Health Association
Factsheet: Stress - Coping With Everyday Problems.
Share your feelings. Stay in touch with friends
and family. Let them provide love, support and
guidance. Do not try to cope alone.
Give in occasionally. Be flexible. If you are
meeting constant opposition in either your
personal or professional life, rethink your position
or strategy. Arguing only intensifies stressful
feelings. If you know you are right, stand your
ground, but do so calmly and rationally. Listen
to the opinions of others and be prepared to
compromise. If you are willing to give in, others
may meet you halfway. Not only will you reduce
your stress; you may find better solutions to
your problems.
Help at home and in your community
Who to call for help
You should contact your surgeon’s office if you
experience any of the following:
Before discharge, your hospital care team will
talk to you about returning home. They will set
up your home care through the Community Care
Access Center (CCAC) in your area. A CCAC
care coordinator may visit you in hospital to talk
about your care plan and will work with you to
develop a personalized care plan that will include
a community Enterostomal Nurse (ET) nurse.
Some patients may return home immediately
and in that case, a CCAC care coordinator and
community nurse will call you within the first few
days following your discharge to discuss your
care plan. The number and frequency of in-home
visits is based on your assessed needs. Your care
coordinator will set up your nursing care and a
schedule that works for you. All Ontario residents
with a valid health card are eligible for home care.
• Temperature or fever of 38.5°C or greater.
• Increased pain or redness along the
incision line.
• Drainage from the incision line.
• Change in the color of the stoma (from red/
pink to grey/dusky or black).
• Cloudy, foul smelling urine, low back pain.
• Prolonged nausea and/or vomiting.
• If you cannot reach your surgeon or family
doctor, and you are in need of medical
assistance, go to your local Emergency
Department.
You should contact your doctor or Enterostomal
Therapy (ET) nurse if you are experiencing any
problems with your stoma, the skin around your
stoma, problems with the pouching system or any
general coping concerns.
Making a follow-up
appointment with
your surgeon
You will need to see your
surgeon within two to
four weeks for a followup appointment after your
surgery. Your hospital care
team may arrange this before
you leave the hospital. If your
appointment is not set up, call your surgeon’s
office to book your appointment.
Purchasing ostomy supplies
There is a wide range of ostomy products
available to you, and your Enterostomal Therapy
(ET) nurse. Your nurse will identify the supplies
that best meet your needs. Before you leave the
hospital, you will receive enough initial supplies
to take home so that you can deal with any
emergency that comes up before your home
care nurse visits you within the first day or two
at home. Your hospital nurse will also order your
first couple of weeks of supplies and have them
delivered to your home for your community nurse
to use during your home visits.
Before discharge, it is important to discuss
financial reimbursement/insurance concerns
and how and where to purchase supplies. Your
Enterostomal Therapy (ET) nurse in the hospital
will work with you to fill out your application for
funding before you leave the hospital.
In Ontario, a person with a permanent ostomy or
an ostomy for more than six months will receive
funding through a program called “Assistive
Devices.” The funding is $600 per year for as long
as the individual has the ostomy. Most people
with an ostomy spend $1000 to $1200 per year
on supplies.
Community support and information
There are numerous resources available
for patients with ostomies. These include
Enterostomal Therapists, support groups and
associations, literature, websites, videos, and
ostomy supplier support. Ostomy manufacturers
provide multiple resources for patients including
videos/DVDs, magazines, booklets, literature,
and ostomy products. Call the 1-800 numbers
for sample products. We have included several of
these resources in this booklet.
Your community nurse will also provide you with
information on where to order additional supplies.
You always want to have enough products
available. It is recommended that you have at
least a one-month supply on hand at all times.
Information on where to buy supplies is located
on page 22.
Resource lists and contacts
Ostomy Supply Manufactures
Name
Hollister Incorporated
Coloplast Canada
Corporation
ConvaTec
Contact Information
95 Mary Street, Aurora, Ontario L4G 1G3
1-800-263-7400
www.hollister.com
3300 Ridgeway Drive, Unit 12, Mississauga, Ontario L5L 5Z9
1-888-880-8605
www.coloplast.com
2365 Cote-de-Liesse, Montréal, Québec H4N 2M7
1-800-465-6302
www.convatec.com
Local Ostomy Suppliers
Name
Shoppers Home Health Care
King Medical Arts Pharmacy
and Home Health Care
First Choice Home Health
Care Inc.
Rexall Pharma Plus - Acton
Campbellville Pharmacy
Guardian Pharmacy Mississauga
Glen Cade Pharmacy
Contact Information
448 Speers Rd., Oakville, Ontario
905-844-1445
www.shoppershomehealthcare.ca
71 King Street W, Mississauga, Ontario
905-270-2226
5130 Dixie Rd, Unit 5, Mississauga, Ontario
905-624-3404
372 Queen Street East, Acton, Ontario
1-877-378-4100
www.rexall.ca
35 Crawford Cres., Campbellville, Ontario
905-854-0313
2180 Credit Valley Road, Mississauga, Ontario
905-820-5434
The West Mall Shopping Centre, 290 The West Mall,
Etobicoke, Ontario
416-622-2111
Please Note: This is not a complete list of local ostomy suppliers in Mississauga Halton. Locations and
contact information may change.
You can find additional Ostomy suppliers at www.mississaugahaltonhealthline.ca under
Ostomy Supplies.
Ostomy Clothing and Accessories
Name
Weir Comfees
Ostomy Secrets
White Rose
Intimate Moments Apparel
Colo-Majic Distribution Canada Ltd.
Vanilla Blush
Contact Information
89A High Street, Aurora, Ontario L4G 1G3
1-800-263-7400
www.weircomfees.com
1-877-613-6246
www.ostomysecrets.com
www.whiterosecollection.com
www.intimatemomentsapparel.com
(flushable liners)
www.colostomymajic.com
www.vblush.com
Financial Assistance and Resources
Resource
Ontario Provincial Government
Assistive Devices Program
(ADP)
Northern and Indian Affairs
Veteran’s Affairs Canada
Contact Information
1-800-567-9604
416-327-8804
www.health.gov.on.ca/en/public/programs/adp
For permanent ostomies or for those who will have an ostomy for
more than six months.
Ontario residents only.
1-800-567-9604
infoPubs@ainc-inac.gc.ca
1-866-522-2122
information@vac-acc.gc.ca
Private Insurance Plans
Tax Credit – request form #T2201 (doctor’s signature is required)
Community Support Groups
Name
United Ostomy Association
of Canada
United Ostomy Association
of Ontario
Contact Information
1-888-969-9698
www.ostomycanada.ca
A support group offering mutual aid and moral support for people
who have had ostomy surgery.
Toronto
416-596-7718
www.ostomytoronto.com
Halton Peel Counties
905-825-3443
Brantford & District
519-752-5037
Hamilton & District
905-542-2386
www.uoaaa.org
GLO Network
Canadian Cancer Society
Support group for gay/lesbian/bisexual ostomates;
their partners; family; caregivers & friends.
1-888-939-3333
www.cancer.ca
Cancer Care Ontario
www.cancercare.on.ca
Bladder Cancer Support Group
www.blcwebcafe.org
Mississauga Halton HealthLine
www.mississaugahaltonhealthline.ca
Health information and resources
Glossary
Enterostomal Therapy (ET) Nurse – Is a
registered nurse with advanced and specialized
knowledge and clinical skills in wound, ostomy
and continence care.
Skin Barrier – Are an important component of
the ostomy pouching system as it protects skin
around the stoma, secures the pouch, and creates
a smooth surface to seat the ostomy pouch.
Flange – The plastic ring in a two-piece ostomy
system that is used to connect the skin barrier and
pouch together.
Stoma – The part of the bowel that is seen outside
of the body on the abdomen following ostomy
surgery. The stoma is pink and moist and doesn’t
have feeling.
Ostomy – A surgically created opening into the
digestive or urinary system, diverting stool or
urine from its normal route
Urostomy – A surgical procedure that creates a
stoma (artificial opening) for the urinary system.
Ostomy pouching system – A prosthetic medical
device that provides a means for the collection
of stool from a surgically diverted biological
system (colon, ileum, bladder) and the creation of
a stoma.
Notes and other important information
(consider including your specific contact names and numbers):

Leaving hospital following urostomy surgery

Transcription

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